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  2. Dimethylamine - Wikipedia

    en.wikipedia.org/wiki/Dimethylamine

    Dimethylamine is an organic compound with the formula (CH 3) 2 NH. This secondary amine is a colorless, flammable gas with an ammonia -like odor. Dimethylamine is commonly encountered commercially as a solution in water at concentrations up to around 40%.

  3. Amine - Wikipedia

    en.wikipedia.org/wiki/Amine

    Amine. In chemistry, amines (/ ə ˈ m iː n, ˈ æ m iː n /, [1] [2] UK also / ˈ eɪ m iː n / [3]) are compounds and functional groups that contain a basic nitrogen atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group [4] (these may respectively be called alkylamines ...

  4. Category:Secondary amines - Wikipedia

    en.wikipedia.org/wiki/Category:Secondary_amines

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  5. File:Stearamidopropyl dimethylamine.png - Wikipedia

    en.wikipedia.org/wiki/File:Stearamidopropyl...

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  6. Dimethylaminopropylamine - Wikipedia

    en.wikipedia.org/wiki/Dimethylaminopropylamine

    DMAPA is commonly produced commercially via the reaction between dimethylamine and acrylonitrile (a Michael reaction) to produce dimethylaminopropionitrile. A subsequent hydrogenation step yields DMAPA: [2] DMAPA is readily converted to the mustard dimethylaminopropyl-3-chloride, a powerful alkylating agent. [3]

  7. Methylamine - Wikipedia

    en.wikipedia.org/wiki/Methylamine

    Methylamine has been produced industrially since the 1920s (originally by Commercial Solvents Corporation for dehairing of animal skins). [4] This was made possible by Kazimierz Smoleński [] and his wife Eugenia who discovered amination of alcohols, including methanol, on alumina or kaolin catalyst after WWI, filed two patent applications in 1919 [5] and published an article in 1921.

  8. N-Nitrosodimethylamine - Wikipedia

    en.wikipedia.org/wiki/N-Nitrosodimethylamine

    NDMA forms from a variety of dimethylamine-containing compounds, e.g. hydrolysis of dimethylformamide. Dimethylamine is susceptible to oxidation to unsymmetrical dimethylhydrazine, which air-oxidizes to NDMA. [15] In the laboratory, NDMA can be synthesised by the reaction of nitrous acid with dimethylamine: HONO + (CH 3) 2 NH → (CH 3) 2 NNO ...

  9. Bis(dimethylamino)methane - Wikipedia

    en.wikipedia.org/wiki/Bis(dimethylamino)methane

    Bis(dimethylamino)methane is the organic compound with the formula [(CH 3) 2 N] 2 CH 2.It is classified as an aminal as well as a ditertiary amine, in fact the simplest.It is a colorless liquid that is widely available.